Canonical Allele Identifier: CA942420065

Gene: HTR3B

Linked Data

• dbSNP Id: rs1950040518
• gnomAD v3: 11-113932067-CATT-C
• gnomAD v4: 11-113932067-CATT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932070_113932072del , CM000673.2:g.113932070_113932072del	GRCh38
NC_000011.9:g.113802792_113802794del , CM000673.1:g.113802792_113802794del	GRCh37
NC_000011.8:g.113308002_113308004del	NCBI36
NG_011483.1:g.32204_32206del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.368+203_368+205del MANE Select	ENSP00000260191.2:n.368+203_368+205del
ENST00000260191.7:c.368+203_368+205del	ENSP00000260191.2:n.368+203_368+205del
ENST00000260191.6:c.368+203_368+205del	ENSP00000260191.2:n.368+203_368+205del
ENST00000537778.5:c.335+203_335+205del	ENSP00000443118.1:n.335+203_335+205del
ENST00000543092.1:c.154+203_154+205del
NM_006028.4:c.368+203_368+205del	NP_006019.1:n.368+203_368+205del
XM_011543063.1:c.335+203_335+205del	XP_011541365.1:n.335+203_335+205del
XM_011543064.1:c.167+203_167+205del	XP_011541366.1:n.167+203_167+205del
XM_011543065.1:c.161+203_161+205del	XP_011541367.1:n.161+203_161+205del
XM_011543066.1:c.335+203_335+205del	XP_011541368.1:n.335+203_335+205del
NM_001363563.1:c.335+203_335+205del	NP_001350492.1:n.335+203_335+205del
XM_017018552.2:c.161+203_161+205del	XP_016874041.1:n.161+203_161+205del
XM_024448767.1:c.74+203_74+205del	XP_024304535.1:n.74+203_74+205del
XR_001748034.2:n.619+203_619+205del
NM_001363563.2:c.335+203_335+205del	NP_001350492.1:n.335+203_335+205del
NM_006028.5:c.368+203_368+205del MANE Select	NP_006019.1:n.368+203_368+205del